CN110327973B - 一种交联降冰片烯共聚物/炭黑三维网络负载铜纳米催化剂及其制备方法与应用 - Google Patents
一种交联降冰片烯共聚物/炭黑三维网络负载铜纳米催化剂及其制备方法与应用 Download PDFInfo
- Publication number
- CN110327973B CN110327973B CN201910683516.3A CN201910683516A CN110327973B CN 110327973 B CN110327973 B CN 110327973B CN 201910683516 A CN201910683516 A CN 201910683516A CN 110327973 B CN110327973 B CN 110327973B
- Authority
- CN
- China
- Prior art keywords
- norbornene copolymer
- copper
- carbon black
- catalyst
- dimensional network
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000010949 copper Substances 0.000 title claims abstract description 99
- 229920001577 copolymer Polymers 0.000 title claims abstract description 73
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims abstract description 71
- 229910052802 copper Inorganic materials 0.000 title claims abstract description 71
- 239000006229 carbon black Substances 0.000 title claims abstract description 54
- 239000011943 nanocatalyst Substances 0.000 title claims abstract description 29
- 238000002360 preparation method Methods 0.000 title claims abstract description 19
- 239000003054 catalyst Substances 0.000 claims abstract description 55
- 238000006243 chemical reaction Methods 0.000 claims abstract description 37
- 239000006185 dispersion Substances 0.000 claims abstract description 8
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 51
- 239000000178 monomer Substances 0.000 claims description 46
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 27
- 239000012295 chemical reaction liquid Substances 0.000 claims description 23
- 238000005406 washing Methods 0.000 claims description 15
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 14
- -1 aldehyde ketones Chemical class 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 14
- 238000003756 stirring Methods 0.000 claims description 14
- 229910000033 sodium borohydride Inorganic materials 0.000 claims description 13
- 239000012279 sodium borohydride Substances 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 11
- 229910052796 boron Inorganic materials 0.000 claims description 11
- 238000002156 mixing Methods 0.000 claims description 11
- 238000001035 drying Methods 0.000 claims description 10
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical class [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- PNPBGYBHLCEVMK-UHFFFAOYSA-N benzylidene(dichloro)ruthenium;tricyclohexylphosphanium Chemical compound Cl[Ru](Cl)=CC1=CC=CC=C1.C1CCCCC1[PH+](C1CCCCC1)C1CCCCC1.C1CCCCC1[PH+](C1CCCCC1)C1CCCCC1 PNPBGYBHLCEVMK-UHFFFAOYSA-N 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 7
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 6
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical group CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 claims description 4
- 238000010791 quenching Methods 0.000 claims description 4
- 230000000171 quenching effect Effects 0.000 claims description 4
- 150000002440 hydroxy compounds Chemical class 0.000 claims description 3
- 239000012298 atmosphere Substances 0.000 claims description 2
- 239000008367 deionised water Substances 0.000 claims description 2
- 229910021641 deionized water Inorganic materials 0.000 claims description 2
- 239000011984 grubbs catalyst Substances 0.000 claims description 2
- 239000011261 inert gas Substances 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 230000001376 precipitating effect Effects 0.000 claims description 2
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 10
- 229910052751 metal Inorganic materials 0.000 abstract description 10
- 239000002184 metal Substances 0.000 abstract description 10
- 239000002105 nanoparticle Substances 0.000 abstract description 6
- 241001424392 Lucia limbaria Species 0.000 abstract 1
- 239000000047 product Substances 0.000 description 14
- 229920000642 polymer Polymers 0.000 description 13
- 238000001914 filtration Methods 0.000 description 11
- 229920000636 poly(norbornene) polymer Polymers 0.000 description 10
- 229910001868 water Inorganic materials 0.000 description 10
- 239000002244 precipitate Substances 0.000 description 8
- 238000007259 addition reaction Methods 0.000 description 6
- 239000012300 argon atmosphere Substances 0.000 description 6
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 6
- 239000012071 phase Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000012046 mixed solvent Substances 0.000 description 5
- 239000012074 organic phase Substances 0.000 description 5
- 238000002390 rotary evaporation Methods 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N anhydrous diethylene glycol Natural products OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 150000001639 boron compounds Chemical class 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 238000004440 column chromatography Methods 0.000 description 3
- 230000001276 controlling effect Effects 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- ZQTYQMYDIHMKQB-UHFFFAOYSA-N exo-norborneol Chemical compound C1CC2C(O)CC1C2 ZQTYQMYDIHMKQB-UHFFFAOYSA-N 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000013557 residual solvent Substances 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 238000007323 disproportionation reaction Methods 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000009776 industrial production Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000004064 recycling Methods 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 238000007142 ring opening reaction Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229960001922 sodium perborate Drugs 0.000 description 2
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- JFARWEWTPMAQHW-DHZHZOJOSA-N (e)-3-(4-bromophenyl)-1-phenylprop-2-en-1-one Chemical compound C1=CC(Br)=CC=C1\C=C\C(=O)C1=CC=CC=C1 JFARWEWTPMAQHW-DHZHZOJOSA-N 0.000 description 1
- DQFBYFPFKXHELB-UHFFFAOYSA-N Chalcone Natural products C=1C=CC=CC=1C(=O)C=CC1=CC=CC=C1 DQFBYFPFKXHELB-UHFFFAOYSA-N 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 description 1
- 239000005750 Copper hydroxide Substances 0.000 description 1
- 238000006069 Suzuki reaction reaction Methods 0.000 description 1
- 238000003917 TEM image Methods 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229910003481 amorphous carbon Inorganic materials 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- SGCLBIRCSTXTIU-UHFFFAOYSA-N boric acid;2,3-dimethylbutane-2,3-diol Chemical compound OB(O)O.CC(C)(O)C(C)(C)O.CC(C)(O)C(C)(C)O SGCLBIRCSTXTIU-UHFFFAOYSA-N 0.000 description 1
- UNXISIRQWPTTSN-UHFFFAOYSA-N boron;2,3-dimethylbutane-2,3-diol Chemical compound [B].[B].CC(C)(O)C(C)(C)O UNXISIRQWPTTSN-UHFFFAOYSA-N 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 235000005513 chalcones Nutrition 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229910001956 copper hydroxide Inorganic materials 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 239000002638 heterogeneous catalyst Substances 0.000 description 1
- 230000003100 immobilizing effect Effects 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 239000002082 metal nanoparticle Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 238000005580 one pot reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- DQFBYFPFKXHELB-VAWYXSNFSA-N trans-chalcone Chemical compound C=1C=CC=CC=1C(=O)\C=C\C1=CC=CC=C1 DQFBYFPFKXHELB-VAWYXSNFSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/06—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing polymers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/64—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by introduction of functional groups containing oxygen only in singly bound form
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/025—Boronic and borinic acid compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
- B01J2231/32—Addition reactions to C=C or C-C triple bonds
- B01J2231/323—Hydrometalation, e.g. bor-, alumin-, silyl-, zirconation or analoguous reactions like carbometalation, hydrocarbation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Catalysts (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
Claims (7)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910683516.3A CN110327973B (zh) | 2019-07-26 | 2019-07-26 | 一种交联降冰片烯共聚物/炭黑三维网络负载铜纳米催化剂及其制备方法与应用 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910683516.3A CN110327973B (zh) | 2019-07-26 | 2019-07-26 | 一种交联降冰片烯共聚物/炭黑三维网络负载铜纳米催化剂及其制备方法与应用 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN110327973A CN110327973A (zh) | 2019-10-15 |
CN110327973B true CN110327973B (zh) | 2021-12-21 |
Family
ID=68147658
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201910683516.3A Active CN110327973B (zh) | 2019-07-26 | 2019-07-26 | 一种交联降冰片烯共聚物/炭黑三维网络负载铜纳米催化剂及其制备方法与应用 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN110327973B (zh) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110339860B (zh) * | 2019-07-29 | 2022-03-01 | 湖北工程学院 | 交联降冰片烯共聚物复合炭黑三维网络固载铂纳米催化剂及其制备方法和应用 |
CN114797976B (zh) * | 2022-04-28 | 2023-11-17 | 湖北工程学院 | 一种交联降冰片烯共聚物/炭黑三维网络固载双金属铜/金纳米催化剂的制备及应用 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10114246A1 (de) * | 2001-03-22 | 2003-07-10 | Schubert Ulrich S | Kontrollierte Radikalische Polymerisation mit Heterogenen Katalysatoren auf Heterocyclen-Metall-Komplex-Basis |
CN104685577A (zh) * | 2012-06-22 | 2015-06-03 | C3奈米有限公司 | 金属纳米结构化网络和透明导电材料 |
CN104959163A (zh) * | 2015-05-19 | 2015-10-07 | 江苏大学 | 一种可控制、可调节的金属纳米粒子负载的聚合物催化剂及其制备方法 |
CN108940199A (zh) * | 2018-07-19 | 2018-12-07 | 深圳市环球绿地新材料有限公司 | 一种通过负载金属的方式改善活性炭吸附性能的方法 |
CN109422874A (zh) * | 2017-08-28 | 2019-03-05 | 中国科学院大连化学物理研究所 | 一种咪唑基交联聚合物负载铜纳米粒子催化剂及制备和应用 |
CN109621961A (zh) * | 2018-11-23 | 2019-04-16 | 南昌大学 | 一种生长二维纳米片原位制备金属高分散催化剂的方法 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10317204B4 (de) * | 2003-04-15 | 2008-04-30 | Oxea Deutschland Gmbh | Carbonsäureester auf Basis von 2-Hydroxymethylnorbornan |
-
2019
- 2019-07-26 CN CN201910683516.3A patent/CN110327973B/zh active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10114246A1 (de) * | 2001-03-22 | 2003-07-10 | Schubert Ulrich S | Kontrollierte Radikalische Polymerisation mit Heterogenen Katalysatoren auf Heterocyclen-Metall-Komplex-Basis |
CN104685577A (zh) * | 2012-06-22 | 2015-06-03 | C3奈米有限公司 | 金属纳米结构化网络和透明导电材料 |
CN104959163A (zh) * | 2015-05-19 | 2015-10-07 | 江苏大学 | 一种可控制、可调节的金属纳米粒子负载的聚合物催化剂及其制备方法 |
CN109422874A (zh) * | 2017-08-28 | 2019-03-05 | 中国科学院大连化学物理研究所 | 一种咪唑基交联聚合物负载铜纳米粒子催化剂及制备和应用 |
CN108940199A (zh) * | 2018-07-19 | 2018-12-07 | 深圳市环球绿地新材料有限公司 | 一种通过负载金属的方式改善活性炭吸附性能的方法 |
CN109621961A (zh) * | 2018-11-23 | 2019-04-16 | 南昌大学 | 一种生长二维纳米片原位制备金属高分散催化剂的方法 |
Non-Patent Citations (1)
Title |
---|
纳米铜催化α,β-不饱和酮β-硼酯化及其产物原位脱硼反应的研究;周新丰;《中国优秀博硕士学位论文全文数据库(硕士) 工程科技Ⅰ辑》;20150615;第15页第1.4节Cu纳米催化剂在有机合成反应中的应用 * |
Also Published As
Publication number | Publication date |
---|---|
CN110327973A (zh) | 2019-10-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA1152485A (en) | Preparation of colloidal dispersions of ruthenium, rhodium, osmium and iridium by the polymer-catalyzed decomposition of carbonyl cluster compounds thereof | |
EP1739104B1 (en) | Polymer-supported metal cluster compositions | |
CN110327973B (zh) | 一种交联降冰片烯共聚物/炭黑三维网络负载铜纳米催化剂及其制备方法与应用 | |
KR102133304B1 (ko) | 5-히드록시메틸퍼퓨랄로부터 2,5-퓨란디메탄올 및 2,5-테트라히드로퓨란 디메탄올의 제조방법 | |
CN104759293B (zh) | 一种以纳米碳为载体的负载型钯催化剂及其制备和应用 | |
CN110327974B (zh) | 一种交联降冰片烯共聚物/炭黑三维网络负载钯纳米催化剂及其制备方法与应用 | |
JP4689691B2 (ja) | 酸化反応用高分子担持金クラスター触媒、それを用いたカルボニル化合物の製法 | |
CN108250331B (zh) | 一种烯烃聚合催化剂载体的组成、制备方法及应用 | |
Fan et al. | Pd/Cu bimetallic catalyst immobilized on PEI capped cellulose-polyamidoamine dendrimer: Synthesis, characterization, and application in Sonogashira reactions for the synthesis of alkynes and benzofurans | |
CN110339860B (zh) | 交联降冰片烯共聚物复合炭黑三维网络固载铂纳米催化剂及其制备方法和应用 | |
CN115650829B (zh) | 一种由生物质酚类化合物光催化制备环己酮类化合物的方法 | |
CN108219038B (zh) | 烷氧基镁颗粒的组份及制备方法 | |
CN109535393B (zh) | 微孔有机聚合物纳米微球的制备方法及其产品 | |
Karimi et al. | Highly dispersed palladium nanoparticles supported on an imidazolium-based ionic liquid polymer: an efficient catalyst for oxidation of alcohols | |
CN114870901B (zh) | 用于烯烃氢甲酰化的双亚磷酸酯聚合物催化剂及其制备方法和应用 | |
CN114797976B (zh) | 一种交联降冰片烯共聚物/炭黑三维网络固载双金属铜/金纳米催化剂的制备及应用 | |
CN114920897A (zh) | 两种氘代聚合物及其制备方法 | |
CN114588940A (zh) | 一种用于酚类化合物加氢的镍基催化剂及其制备方法和应用 | |
US4252674A (en) | Preparation of colloidal cobalt dispersions by the polymer-catalyzed decomposition of cobalt carbonyl and cobalt organocarbonyl compounds | |
Al-Kharusi et al. | Synthesis, thin-film self-assembly, and pyrolysis of ruthenium-containing polyferrocenylsilane block copolymers | |
CN115646495B (zh) | 一种高活性NiCu/Al2O3催化剂的制备及其在芳醚C-O键催化氢转移裂解方面的应用 | |
CN108017735B (zh) | 一种球形烷氧基镁颗粒的组份及制备方法 | |
CN107715917A (zh) | 含磷酸***联聚合物负载钯纳米催化剂及制备和应用 | |
CN112047813B (zh) | 一种2,2,4,4-四甲基-1,3-环丁二醇的生产方法 | |
CN114534793B (zh) | 一种三苯基膦聚合物负载型催化剂及制备方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
EE01 | Entry into force of recordation of patent licensing contract | ||
EE01 | Entry into force of recordation of patent licensing contract |
Application publication date: 20191015 Assignee: Hangzhou Hongshun Pipe Industry Co.,Ltd. Assignor: HUBEI ENGINEERING University Contract record no.: X2023980048834 Denomination of invention: A cross-linked norbornene copolymer/carbon black three-dimensional network loaded copper nanocatalyst and its preparation method and application Granted publication date: 20211221 License type: Common License Record date: 20231130 |